Platinum single-atom and cluster catalysis of the hydrogen evolution reaction
Niancai Cheng,
Samantha Stambula,
Da Wang,
Mohammad Norouzi Banis,
Jian Liu,
Adam Riese,
Biwei Xiao,
Ruying Li,
Tsun-Kong Sham,
Li-Min Liu (),
Gianluigi A. Botton () and
Xueliang Sun ()
Additional contact information
Niancai Cheng: University of Western Ontario
Samantha Stambula: McMaster University
Da Wang: Beijing Computational Science Research Center
Mohammad Norouzi Banis: University of Western Ontario
Jian Liu: University of Western Ontario
Adam Riese: University of Western Ontario
Biwei Xiao: University of Western Ontario
Ruying Li: University of Western Ontario
Tsun-Kong Sham: University of Western Ontario
Li-Min Liu: Beijing Computational Science Research Center
Gianluigi A. Botton: McMaster University
Xueliang Sun: University of Western Ontario
Nature Communications, 2016, vol. 7, issue 1, 1-9
Abstract:
Abstract Platinum-based catalysts have been considered the most effective electrocatalysts for the hydrogen evolution reaction in water splitting. However, platinum utilization in these electrocatalysts is extremely low, as the active sites are only located on the surface of the catalyst particles. Downsizing catalyst nanoparticles to single atoms is highly desirable to maximize their efficiency by utilizing nearly all platinum atoms. Here we report on a practical synthesis method to produce isolated single platinum atoms and clusters using the atomic layer deposition technique. The single platinum atom catalysts are investigated for the hydrogen evolution reaction, where they exhibit significantly enhanced catalytic activity (up to 37 times) and high stability in comparison with the state-of-the-art commercial platinum/carbon catalysts. The X-ray absorption fine structure and density functional theory analyses indicate that the partially unoccupied density of states of the platinum atoms’ 5d orbitals on the nitrogen-doped graphene are responsible for the excellent performance.
Date: 2016
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms13638
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DOI: 10.1038/ncomms13638
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